MY ESSENTIALS CITRUS SCENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]

MY ESSENTIALS CITRUS SCENT (TRICLOSAN) SOAP [SUN PRODUCTS CORPORATION]
PDF | XML

NDC	63691-022-04
Set ID	ac232de0-aee2-4774-a1e9-88ec5760fe7a
Category	HUMAN OTC DRUG LABEL
Packager	Sun Products Corporation
Generic Name
Product Class
Product Number
Application Number	PART333E

View All Sections

ACTIVE INGREDIENT

Active ingredient

Triclosan 0.10%

Use helps fight germs on hands when used as a hand soap

For external use only

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. In case of eye contact, rinse thoroughly with water.

Directions wash hands and rinse

Antibacterial hand soap

Inactive ingredients Water, Sodium Dodecylbenzenesulfonate, Palm Kernelamide DEA, Sodium Methyl 2-Sulfopalmitate, Urea, Sodium Chloride, Disodium 2-Sulfopalmitate, Methyl Palmitate, Fragrance, Sodium Citrate, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, D&C Orange No. 4

Questions? 1-866-322-2439
PRINCIPAL DISPLAY PANEL

LBLFR

LBLBK

INGREDIENTS AND APPEARANCE

MY ESSENTIALS CITRUS SCENT
triclosan soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:63691-022
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.1 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
UREA (UNII: 8W8T17847W)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DISODIUM 2-SULFOPALMITATE (UNII: VS9295575T)
METHYL PALMITATE (UNII: DPY8VCM98I)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SULISOBENZONE (UNII: 1W6L629B4K)
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:63691-022-04	739 mL in 1 BOTTLE

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	07/01/2014

Labeler - Sun Products Corporation (070931480)

View All Sections

Related Drugs